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Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia

27 August 2016 (00:00 - 00:00)
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Congress Presentation Part of: Poster session 4 - Miscellaneous in arrhythmia Genetic aspects of arrhythmias ESC Premium Access ESC Congress 2016

About the speaker

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Doctor Seiko Ohno

National Cerebral & Cardiovascular Center, Suita (Japan)

28 More presentations in this session

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A novel CACNA1C mutation identified in a patient with atypical Timothy syndrome exerts both loss- and gain-of-function effects on Cav1.2.
Doctor J. Ozawa (Niigata, JP)
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Genetic testing in a consecutive series of young athletes with suspected cathecolaminargic polymorphic ventricular tachycardia
Associate Professor N. Marziliano (Garbagnate Milanese, IT)
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The burden of complex arrhythmic genotypes in a consecutive series of Sardinian population of patients with primary arrhythmic disorders
Associate Professor N. Marziliano (Garbagnate Milanese, IT)
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Discrepancy of QTc duration and LQTS risk score for the diagnosis of type 3 LQTS
Doctor A. Hermida (Paris, FR)
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Complex inherited cardiac diseases inheritance in a family harbouring compound SCN5A and MYBPC3 mutations.
Doctor R. Mango (Rome, IT)
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Poster session 4 - Miscellaneous in arrhythmia

The Event

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ESC Congress 2016

27 August - 31 August 2016

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources